14 results · 17ms · Sources: EU EUDAMED, US FDA

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Burst Suppression Detection Software For Electroencephalograph

FDA classification
FDA Class 2 ·Burst Suppression Detection Software For Electroencephalograph

Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

FDA classification
FDA Class 2 ·Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

Restraint, Patient, Conductive

FDA classification
FDA Class 1 ·Restraint, Patient, Conductive

Leadless Cardiac Resynchronization Therapy (Crt)

FDA classification
FDA Class 3 ·Leadless Cardiac Resynchronization Therapy (Crt)

Implantable Cardioverter Defibrillator (Non-Crt)

FDA classification
FDA Class 3 ·Implantable Cardioverter Defibrillator (Non-Crt)

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA classification
FDA Class 3 ·Implantable Pulse Generator, Pacemaker (Non-Crt)

Pacemaker/Icd/Crt Non-Implanted Components

FDA classification
FDA Class 3 ·Pacemaker/Icd/Crt Non-Implanted Components

System, Imaging, Optical Coherence Tomography (Oct)

FDA classification
FDA Class 2 ·System, Imaging, Optical Coherence Tomography (Oct)

Television Or Monitor, Non-Crt, Non-Medical, Video Display

FDA classification
FDA Not Classified ·Television Or Monitor, Non-Crt, Non-Medical, Video Display

Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

FDA classification
FDA Class 3 ·Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

FDA classification
FDA Class 3 ·Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

Home Monitoring Ophthalmic Optical Coherence Tomography (Oct) Imaging Device

FDA classification
FDA Class 2 ·Home Monitoring Ophthalmic Optical Coherence Tomography (Oct) Imaging Device

Oct Imaging System With Ai/Ml Software For Adjunctive Detection Of Breast Cancer

FDA classification
FDA Class 3 ·Oct Imaging System With Ai/Ml Software For Adjunctive Detection Of Breast Cancer

Multiplex Immunoassay For T. Gondii, Rubella, Cytomegalovirus And Herpes Simplex Virus 1 And 2

FDA classification
FDA Class 2 ·Multiplex Immunoassay For T. Gondii, Rubella, Cytomegalovirus And Herpes Simplex Virus 1 And 2